ID

27479

Description

Swedish Bladder Cancer Registry Healthcare Quality http://www.cancercentrum.se/vast/cancerdiagnoser/urinvagar/urinblase--och-urinvagscancer/kvalitetsregister/dokument/ Treatment of Primary Tumor

Link

http://www.cancercentrum.se/vast/cancerdiagnoser/urinvagar/urinblase--och-urinvagscancer/kvalitetsregister/dokument/

Keywords

  1. 11/15/17 11/15/17 -
Copyright Holder

Regionalt CancerCentrum Väst

Uploaded on

November 15, 2017

DOI

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License

Creative Commons BY-NC-ND 3.0

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Swedish Bladder Cancer Registry

Treatment of Primary Tumor

General Information
Description

General Information

Alias
UMLS CUI-1
C0034975
The form must be completed and submitted to: Regional Cancer Centre in each region.
Description

Cancer Centre

Data type

text

Alias
UMLS CUI [1]
C1301943
Physician
Description

Physician

Data type

text

Alias
UMLS CUI [1]
C2826892
Hospital/Clinic
Description

Hospital

Data type

text

Alias
UMLS CUI [1]
C0019994
Date of Report
Description

Date of Report

Data type

date

Measurement units
  • yy-mm-dd
Alias
UMLS CUI [1]
C1302584
yy-mm-dd
Patient-No.: (yyyy-mm-dd-xxxx)
Description

Patient ID

Data type

text

Alias
UMLS CUI [1]
C2348585
Name
Description

Patient's Name

Data type

text

Alias
UMLS CUI [1]
C1299487
Treatment of Primary Tumor - To be completed after completion of primary treatment (regardless of time interval)
Description

Treatment of Primary Tumor - To be completed after completion of primary treatment (regardless of time interval)

Alias
UMLS CUI-1
C0086143
UMLS CUI-2
C0332137
Patient has designated contact nurse?
Description

Contact Nurse

Data type

boolean

Alias
UMLS CUI [1]
C0583629
Chemotherapy Single Shot?
Description

Chemotherapy Single Shot

Data type

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C1301654
Resection?
Description

Bladder Resection

Data type

boolean

Alias
UMLS CUI [1]
C0194386
Resection? If yes, specify date of resection:
Description

Date of Bladder Resection

Data type

date

Measurement units
  • yy-mm-dd
Alias
UMLS CUI [1,1]
C0194386
UMLS CUI [1,2]
C0011008
yy-mm-dd
If there was a resection, was the detrusor in the preparation?
Description

Bladder Resection: Detrusor

Data type

boolean

Alias
UMLS CUI [1,1]
C0194386
UMLS CUI [1,2]
C1180419
Clinical Stage: T-stage (TNM-2009)
Description

T-stage (UICC: TNM-classification 2009) Tis: Non-invasive flat carcinoma (flat, non-exofytic tumor) Ta: Non-invasive papillary carcinoma T1: The tumor has grown from the layer of cells lining the bladder into the connective tissue below. T2: superficial muscle <1/2 and deep muscle> 1/2 T3: extravesical. resistance / macroscopic and perivesic / microscopic T4: T4a: The tumor has spread to the stroma of the prostate (in men), or to the uterus and/or vagina (in women). T4b: The tumor has spread to the pelvic wall or the abdominal wall. Tx: Criteria not met

Data type

text

Alias
UMLS CUI [1,1]
C0475455
UMLS CUI [1,2]
C0005684
Clinical Stage: Grade (WHO 1999)
Description

Grading (WHO 1999): LMP: Urothelial neoplasm of low malignancy potential G1: Urothelial cancer grade I G2: Urothelial cancer grade II G3: Urothelial cancer grade III GX: Differentiation can not be estimated

Data type

text

Alias
UMLS CUI [1,1]
C0441800
UMLS CUI [1,2]
C0005684
Discussed at multidisciplinary conference?
Description

Tumor Conference

Data type

boolean

Alias
UMLS CUI [1]
C2985541
Participation in Clinical Trial?
Description

Study Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
Further Treatment?
Description

If no further treatment is given, the form is completed and can be sent to the regional cancer center.

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C1517331
Intravesical Treatment?
Description

Intravesical Treatment

Data type

boolean

Alias
UMLS CUI [1]
C0444473
Intravesical Treatment? If YES, specify Start Date:
Description

Intravesical Treatment: Start Date

Data type

date

Measurement units
  • yy-mm-dd
Alias
UMLS CUI [1,1]
C0444473
UMLS CUI [1,2]
C0808070
yy-mm-dd
Intravesical Treatment? If YES, specify the treatment:
Description

Intravesical Treatment: Specification

Data type

text

Alias
UMLS CUI [1,1]
C0444473
UMLS CUI [1,2]
C0808070
UMLS CUI [1,3]
C2348235
Systemic Chemotherapy?
Description

Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
Neoadjuvant?
Description

Neoadjuvant Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0600558
Induction?
Description

Induction Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C3179010
Adjuvant?
Description

Adjuvant Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0085533
Palliative Care?
Description

Palliative Care

Data type

boolean

Alias
UMLS CUI [1]
C0030231
Treating Hospital for Chemotherapy:
Description

Hospital for Chemotherapy

Data type

text

Alias
UMLS CUI [1,1]
C0019994
UMLS CUI [1,2]
C0392920
Cystectomy?
Description

Cystectomy complication registration in INCA - mandatory from 01/01/2011

Data type

boolean

Alias
UMLS CUI [1]
C0010651
Treating Hospital for Cystectomy:
Description

Cystectomy complication registration in INCA - mandatory from 01/01/2011

Data type

text

Alias
UMLS CUI [1,1]
C0019994
UMLS CUI [1,2]
C0010651
Radiation with curative intention?
Description

Radiation: Curative Intention

Data type

boolean

Alias
UMLS CUI [1,1]
C0851346
UMLS CUI [1,2]
C1276305
Radiation with curative intention? If YES, specify the start date:
Description

Radiation: Start Date

Data type

date

Measurement units
  • yy-mm-dd
Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0808070
yy-mm-dd
Radiation with curative intention? If Yes, please specify the treating hospital:
Description

Hospital for Radiation

Data type

text

Alias
UMLS CUI [1,1]
C0851346
UMLS CUI [1,2]
C0019994

Similar models

Treatment of Primary Tumor

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
General Information
C0034975 (UMLS CUI-1)
Cancer Centre
Item
The form must be completed and submitted to: Regional Cancer Centre in each region.
text
C1301943 (UMLS CUI [1])
Physician
Item
Physician
text
C2826892 (UMLS CUI [1])
Hospital
Item
Hospital/Clinic
text
C0019994 (UMLS CUI [1])
Date of Report
Item
Date of Report
date
C1302584 (UMLS CUI [1])
Patient ID
Item
Patient-No.: (yyyy-mm-dd-xxxx)
text
C2348585 (UMLS CUI [1])
Patient's Name
Item
Name
text
C1299487 (UMLS CUI [1])
Item Group
Treatment of Primary Tumor - To be completed after completion of primary treatment (regardless of time interval)
C0086143 (UMLS CUI-1)
C0332137 (UMLS CUI-2)
Contact Nurse
Item
Patient has designated contact nurse?
boolean
C0583629 (UMLS CUI [1])
Chemotherapy Single Shot
Item
Chemotherapy Single Shot?
boolean
C0392920 (UMLS CUI [1,1])
C1301654 (UMLS CUI [1,2])
Bladder Resection
Item
Resection?
boolean
C0194386 (UMLS CUI [1])
Date of Bladder Resection
Item
Resection? If yes, specify date of resection:
date
C0194386 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Bladder Resection: Detrusor
Item
If there was a resection, was the detrusor in the preparation?
boolean
C0194386 (UMLS CUI [1,1])
C1180419 (UMLS CUI [1,2])
Item
Clinical Stage: T-stage (TNM-2009)
text
C0475455 (UMLS CUI [1,1])
C0005684 (UMLS CUI [1,2])
Code List
Clinical Stage: T-stage (TNM-2009)
CL Item
T1 (lamina propria) (T1 (lamina propria))
CL Item
Ta (ej invasiv) (Ta (ej invasiv))
CL Item
T2 (ytlig muskel <1/2 och djup muskel >1/2) (T2 (ytlig muskel <1/2 och djup muskel >1/2))
CL Item
T3 (extravesical. resistens/makroskopisk och perivesic/mikroskopisk) (T3 (extravesical. resistens/makroskopisk och perivesic/mikroskopisk))
CL Item
TX (kriterier ej uppfyllda) (TX (kriterier ej uppfyllda))
CL Item
T0 (no tumor) (T0 (no tumor))
CL Item
Tis (endast primär, in situ) (Tis (endast primär, in situ))
CL Item
T4a (prostata/vagina, uterus) T4b (bäckenvägg, bukvägg, rektum) (T4a (prostata/vagina, uterus) T4b (bäckenvägg, bukvägg, rektum))
Item
Clinical Stage: Grade (WHO 1999)
text
C0441800 (UMLS CUI [1,1])
C0005684 (UMLS CUI [1,2])
Code List
Clinical Stage: Grade (WHO 1999)
CL Item
LMP (LMP)
CL Item
G1 (G1)
CL Item
G2 (G2)
CL Item
G3 (G3)
CL Item
GX (GX)
Tumor Conference
Item
Discussed at multidisciplinary conference?
boolean
C2985541 (UMLS CUI [1])
Study Participation Status
Item
Participation in Clinical Trial?
boolean
C2348568 (UMLS CUI [1])
Further Treatment
Item
Further Treatment?
boolean
C0087111 (UMLS CUI [1,1])
C1517331 (UMLS CUI [1,2])
Intravesical Treatment
Item
Intravesical Treatment?
boolean
C0444473 (UMLS CUI [1])
Intravesical Treatment: Start Date
Item
Intravesical Treatment? If YES, specify Start Date:
date
C0444473 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Item
Intravesical Treatment? If YES, specify the treatment:
text
C0444473 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
Code List
Intravesical Treatment? If YES, specify the treatment:
CL Item
BCG (BCG)
CL Item
 (Cytostatika – flergångsinstillation)
Chemotherapy
Item
Systemic Chemotherapy?
boolean
C0392920 (UMLS CUI [1])
Neoadjuvant Chemotherapy
Item
Neoadjuvant?
boolean
C0600558 (UMLS CUI [1])
Induction Chemotherapy
Item
Induction?
boolean
C3179010 (UMLS CUI [1])
Adjuvant Chemotherapy
Item
Adjuvant?
boolean
C0085533 (UMLS CUI [1])
Palliative Care
Item
Palliative Care?
boolean
C0030231 (UMLS CUI [1])
Hospital for Chemotherapy
Item
Treating Hospital for Chemotherapy:
text
C0019994 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Cystectomy
Item
Cystectomy?
boolean
C0010651 (UMLS CUI [1])
Hospital for Cystectomy
Item
Treating Hospital for Cystectomy:
text
C0019994 (UMLS CUI [1,1])
C0010651 (UMLS CUI [1,2])
Radiation: Curative Intention
Item
Radiation with curative intention?
boolean
C0851346 (UMLS CUI [1,1])
C1276305 (UMLS CUI [1,2])
Radiation: Start Date
Item
Radiation with curative intention? If YES, specify the start date:
date
C1522449 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Hospital for Radiation
Item
Radiation with curative intention? If Yes, please specify the treating hospital:
text
C0851346 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])

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